A Pathway for Phosphatidylcholine Biosynthesis in Plasmodium falciparum Involving Phosphoethanolamine Methylation

• Published in: Proceedings of the National Academy of Sciences - PNAS 2004-04, Vol.101 (16), p.6206-6211
• Main Authors: Pessi, Gabriella, Kociubinski, Guillermo, Ben Mamoun, Choukri, Borst, P.
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Animals; Base Sequence; Biological Sciences; Biosynthesis; Chemotherapy; DNA Primers; Enzymes; Erythrocytes; Lipids; Malaria; Methylation; Methyltransferases - chemistry; Methyltransferases - metabolism; Microbiology; Molecular Sequence Data; Parasites; Parasitism; Phosphatidylcholines; Phosphatidylcholines - biosynthesis; Phosphatidylethanolamine N-Methyltransferase; Phosphatidylethanolamines - metabolism; Phospholipids; Plasmodium falciparum; Plasmodium falciparum - enzymology; Plasmodium falciparum - metabolism; Proteins; Recombinant Proteins - chemistry; Recombinant Proteins - metabolism; Sequence Homology, Amino Acid
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.0307742101

Plasmodium falciparum is the causative agent of the most severe form of human malaria. The rapid multiplication of the parasite within human erythrocytes requires an active production of new membranes. Phosphatidylcholine is the most abundant phospholipid in Plasmodium membranes, and the pathways leading to its synthesis are attractive targets for chemotherapy. In addition to its synthesis from choline, phosphatidylcholine is synthesized from serine via an unknown pathway. Serine, which is actively transported by Plasmodium from human serum and readily available in the parasite, is subsequently converted into phosphoethanolamine. Here, we describe in P. falciparum a plant-like S-adenosyl-L-methionine-dependent three-step methylation reaction that converts phosphoethanolamine into phosphocholine, a precursor for the synthesis of phosphatidylcholine. We have identified the gene, PfPMT, encoding this activity and shown that its product is an unusual phosphoethanolamine methyltransferase with no human homologs. P. falciparum phosphoethanolamine methyltransferase (Pfpmt) is a monopartite enzyme with a single catalytic domain that is responsible for the three-step methylation reaction. Interestingly, Pfpmt activity is inhibited by its product phosphocholine and by the phosphocholine analog, miltefosine. We show that miltefosine can also inhibit parasite proliferation within human erythrocytes. The importance of this enzyme in P. falciparum membrane biogenesis makes it a potential target for malaria chemotherapy.